ClearanceBrief
510(k) K000009 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

SPIRAL RADIUS RODDING SYSTEM

ApplicantUnited States Surgical, A Division of Tyco Healthc, Norwalk CT, US
DecisionSubstantially Equivalent, Mar 10, 2000
ReceivedJan 3, 2000
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K000009

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.